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Variant : CV162623 (GRCh38/hg38 8p23.1(chr8:8253505-11422633)x1) Homo sapiens

Symbol: CV162623
Name: GRCh38/hg38 8p23.1(chr8:8253505-11422633)x1
Condition: See cases [RCV000141377]
Clinical Significance: pathogenic
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC022784.1   AC104964.1   AC105001.1   AF131215.3   AF131216.3   C8orf74   CLDN23   ERI1   FAM167A   FAM167A-AS1   MFHAS1   MIR124-1   MIR124-1HG   MIR1322   MIR4286   MIR4660   MIR597   MIR598   MSRA   MTMR9   PINX1   PPP1R3B   PRAG1   PRSS51   PRSS55   RP1L1   SLC35G5   SNORD3I   SOX7   TNKS   XKR6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_8253505)_(11422633_?)del
NC_000008.10:g.(?_8111027)_(11280142_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3888,253,505 - 11,422,633CLINVAR
GRCh3788,111,027 - 11,280,142CLINVAR
Build 3688,148,437 - 11,317,552CLINVAR
Cytogenetic Map88p23.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488902
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.